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openAccessImage1_Expanding the phenotype of THRB_ a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing varia.PDF.jpg21-jul-2023Image1_Expanding the phenotype of THRB: a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing variant.PDFFernández-Suárez, Elena CSIC ORCID; González del Pozo, María CSIC ORCID; García-Núñez, Alejandro; Méndez-Vidal, Cristina CSIC ORCID; Martín-Sánchez, Marta CSIC ORCID; Mejías-Carrasco, José Manuel; Ramos-Jiménez, Manuel; Morillo-Sánchez, María José; Rodríguez-de-la-Rúa-Franch, Enrique; Borrego, Salud CSIC ORCID; Antiñolo, Guillermo CSIC ORCIDdataset
openAccesssrep23910.pdf.jpg1-abr-2016Improving the management of Inherited Retinal Dystrophies by targeted sequencing of a population-specific gene panelBravo-Gil, Nereida CSIC; Méndez-Vidal, Cristina CSIC ORCID; Romero-Pérez, Laura CSIC ORCID; González del Pozo, María CSIC ORCID; Rodríguez-de-la-Rúa-Franch, Enrique; Dopazo, Joaquín CSIC ORCID; Borrego, Salud CSIC ORCID; Antiñolo, Guillermo CSIC ORCIDartículo
openAccessMalignant_transformation_2009.pdf.jpg15-jul-2009Induction of Dlk1 by PTTG1 Inhibits Adipocyte Differentiation and Correlates with Malignant TransformationEspina, Águeda G. CSIC; Méndez-Vidal, Cristina CSIC ORCID; Moreno-Mateos, Miguel A. CSIC ORCID; Sáez, Carmen CSIC ORCID; Romero-Franco, Ana CSIC; Japón, Miguel A. CSIC ORCID; Pintor-Toro, José Antonio CSIC ORCIDartículo
openAccessspectrum_semaphorin_3A_Luzon.pdf.PDF.jpg23-ene-2013Mutational Spectrum of Semaphorin 3A and Semaphorin 3D Genes in Spanish Hirschsprung patientsLuzón-Toro, Berta CSIC; Fernández, Raquel M. CSIC ORCID; Torroglosa, Ana CSIC ORCID; Agustín, Juan Carlos de; Méndez-Vidal, Cristina CSIC ORCID; Segura, Dolores Isabel; Antiñolo, Guillermo CSIC ORCID; Borrego, Salud CSIC ORCIDartículo
openAccessNovel_small_RNA_MorenoMateos.pdf.jpg15-oct-2013Novel small RNA expression libraries uncover hsa-miR-30b and hsa-miR-30c as important factors in anoikis resistanceMoreno-Mateos, Miguel A. CSIC ORCID; Barragán, Verónica CSIC; Torres, Belén CSIC; Rodríguez-Mateo, Cristina CSIC ORCID; Méndez-Vidal, Cristina CSIC ORCID; Berezikov, Eugene; Mudduluru, Giridhar; Allgayer, Heike; Pintor-Toro, José Antonio CSIC ORCIDartículo
openAccess3-may-2012Novel small RNAs expresión libraries uncover hsa-mir30c and hsa-mir30b as key factors in anoikis resistanceMoreno-Mateos, Miguel A. CSIC ORCID; Barragán, Verónica CSIC; Torres, Belén CSIC; Méndez-Vidal, Cristina CSIC ORCID; Pintor-Toro, José Antonio CSIC ORCIDpóster de congreso
openAccessPTTG2_silencing_results_MendezVidal.pdf.jpg7-mar-2013PTTG2 silencing results in induction of epithelial-to-mesenchymal transition and apoptosisMéndez-Vidal, Cristina CSIC ORCID; Gámez del Estal, María del Mar CSIC; Moreno-Mateos, Miguel A. CSIC ORCID; Espina, Águeda G. CSIC; Torres, Belén CSIC; Pintor-Toro, José Antonio CSIC ORCIDartículo
openAccessLibroAbstractsSEBC2011_85.pdf.jpg12-dic-2011PTTG2 Silencing results in loss of cell adhesion and apoptosis in adenocarcinoma HCT116 cellsGámez del Estal, María del Mar CSIC; Méndez-Vidal, Cristina CSIC ORCID; Pintor-Toro, José Antonio CSIC ORCIDcomunicación de congreso
openAccesss41598-018-31511-5.pdf.jpg6-sep-2018Searching the second hit in patients with inherited retinal dystrophies and monoallelic variants in ABCA4, USH2A and CEP290 by whole-gene targeted sequencingGonzález del Pozo, María CSIC ORCID; Martín-Sánchez, Marta CSIC ORCID; Bravo-Gil, Nereida CSIC; Méndez-Vidal, Cristina CSIC ORCID; Chimenea, Ángel CSIC ORCID; Rodríguez-de-la-Rúa-Franch, Enrique; Borrego, Salud CSIC ORCID; Antiñolo, Guillermo CSIC ORCIDartículo
openAccess21-jul-2023Table1_Expanding the phenotype of THRB: a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing variant.XLSXFernández-Suárez, Elena CSIC ORCID; González del Pozo, María CSIC ORCID; García-Núñez, Alejandro; Méndez-Vidal, Cristina CSIC ORCID; Martín-Sánchez, Marta CSIC ORCID; Mejías-Carrasco, José Manuel; Ramos-Jiménez, Manuel; Morillo-Sánchez, María José; Rodríguez-de-la-Rúa-Franch, Enrique; Borrego, Salud CSIC ORCID; Antiñolo, Guillermo CSIC ORCIDdataset
openAccessTable2_Expanding the phenotype of THRB_ a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing varia.PDF.jpg21-jul-2023Table2_Expanding the phenotype of THRB: a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing variant.PDFFernández-Suárez, Elena CSIC ORCID; González del Pozo, María CSIC ORCID; García-Núñez, Alejandro; Méndez-Vidal, Cristina CSIC ORCID; Martín-Sánchez, Marta CSIC ORCID; Mejías-Carrasco, José Manuel; Ramos-Jiménez, Manuel; Morillo-Sánchez, María José; Rodríguez-de-la-Rúa-Franch, Enrique; Borrego, Salud CSIC ORCID; Antiñolo, Guillermo CSIC ORCIDdataset
openAccessTable3_Expanding the phenotype of THRB_ a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing varia.pdf.jpg21-jul-2023Table3_Expanding the phenotype of THRB: a range of macular dystrophies as the major clinical manifestations in patients with a dominant splicing variant.pdfFernández-Suárez, Elena CSIC ORCID; González del Pozo, María CSIC ORCID; García-Núñez, Alejandro; Méndez-Vidal, Cristina CSIC ORCID; Martín-Sánchez, Marta CSIC ORCID; Mejías-Carrasco, José Manuel; Ramos-Jiménez, Manuel; Morillo-Sánchez, María José; Rodríguez-de-la-Rúa-Franch, Enrique; Borrego, Salud CSIC ORCID; Antiñolo, Guillermo CSIC ORCIDdataset
openAccessoligogenic_variants.pdf.jpg12-feb-2020Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variantsGonzález del Pozo, María CSIC ORCID; Fernández-Suárez, Elena CSIC ORCID; Martín-Sánchez, Marta CSIC ORCID; Bravo-Gil, Nereida CSIC; Méndez-Vidal, Cristina CSIC ORCID; Rodríguez-de-la-Rúa-Franch, Enrique; Borrego, Salud CSIC ORCID; Antiñolo, Guillermo CSIC ORCIDartículo
openAccesssrep41937.pdf.jpg3-feb-2017Unravelling the genetic basis of simplex Retinitis Pigmentosa casesBravo-Gil, Nereida CSIC; González del Pozo, María CSIC ORCID; Martín-Sánchez, Marta CSIC ORCID; Méndez-Vidal, Cristina CSIC ORCID; Rodríguez-de-la-Rúa-Franch, Enrique; Borrego, Salud CSIC ORCID; Antiñolo, Guillermo CSIC ORCIDartículo
openAccessStargardt_disease.pdf.jpg23-jul-2021Unusual clinical phenotype of Stargardt diseaseMolina-Solana, Pedro; Morillo-Sánchez, María José; Méndez-Vidal, Cristina CSIC ORCID; Ramos-Jiménez, Manuel; Domínguez-Serrano, Francisco de Borja; Antiñolo, Guillermo CSIC ORCID; Rodríguez-de-la-Rúa-Franch, Enriqueartículo